Antifungal activity of trihalogenmethylthio compounds in controlled release paints
Read Online

Antifungal activity of trihalogenmethylthio compounds in controlled release paints by Jennifer Ann Gifford

  • 209 Want to read
  • ·
  • 49 Currently reading

Published by University of Birmingham in Birmingham .
Written in English

Book details:

Edition Notes

Thesis (M.Sc.) - University of Birmingham, School of Biological Sciences, Faculty of Science, 1995.

Statementby Jennifer Ann Gifford.
ID Numbers
Open LibraryOL17326975M

Download Antifungal activity of trihalogenmethylthio compounds in controlled release paints


Antifungal activities were examined and compared for some 40 kinds of aliphatic and aromatic aldehydes, alcohols, phenolic compounds, ether compounds and . Most of the compounds were sesquiterpenes known as antifungal chemicals (i.e aromanderen, element, cadinene, and 2-Octanone), monoterpene (limonene and bisnorhopane), and fatty acids (oleic acid, and monopalmtin). Other VOCs were identified having antifungal activity and plant growth promoters such as caryophyllene and by: 1. On the basis of the above, the objective was to analyze the in vitro antifungal activity of the 3,4,5-trihydrox- ybenzoic and 3,4,5-tris(acetyloxy)benzoic acids, and to calculate their LD 2. Methods Fungal Organisms and Artemia salina The antifungal activity of the compounds was evaluated against eight yeasts of the species Candida. 58 antifungal activity. The extract of Azadirachta indica showed maximum activity; while minimum activity was observed with Holoptelia integrifolia against the test fungi (Pawar, ). The aqueous and different solvent extracts of Cardiospermum halicacabum L. were screened by Girish et al., () for antifungal against a wide array of seed-borne phytopathogenic fungi.

Evaluation of Antifungal Activity on 83 the Fractions obtained from Liquid-liquid Partitioning Bioactivity-guided Fractionation of the Bioactive Fraction 84 of N. gracilis Purification of Compound B 1 from N. gracilis 86 HPTLC Analysis of the Isolated 86 Antifungal Compound B 1. The antifungal activity for both the compounds was better at pH than pH Addition of carvacrol and thymol (64 mg/mL) in red wine resulted in inhibition of growth of the effect on the tested strains at pH due to no release of molecular SO2. At pH , potassium metabisulphite exhibited antifungal ac-. anti-ulcer, antidiabetic and antifungal (Bruneton et al., ). Cinnamaldehye is the most prevalent with concentration of 6, –30, ppm13, The aims of this study were analysis of chemical compounds of Cinnamomum Zeylanicum (Cinnamon bark) and evaluation of antifungal and antibacterial activity. MATERIALS ANd METHOdS. The coumarins (phenolic compounds which possess a benzopyranone nucleus and are one of the major classes of secondary metabolites) have been highlighted in antimicrobial activity studies [6–8]. Recently reported by our group, the antifungal activity against Aspergillus fumigatus and A. flavus of twenty-four coumarin derivatives was described.

ANTIFUNGAL ACTIVITY OF MEDICINAL PLANT EXTRACTS AGAINST PHYTOPATHOGENIC FUNGUS Alternaria SPP. Paola Díaz Dellavalle1, Andrea Cabrera 1, Diego Alem 1, Patricia Larrañaga1, Fernando Ferreira2, and Marco Dalla Rizza1* ABSTRACT The aim of the study was to evaluate the antifungal activity of extracts of 10 plant species used in traditional Uruguayan. The emergence of alternative medicine as a hot field of research has also increased the list of available antifungal compounds. For example, numerous compounds and essential oils found in nature have been found to have antifungal properties that could be utilized for treatment. Examples of these include coconut oil, orange oil, olive leaf, and. In order to quantify the antifungal activity of the commercial facade paints, a specifically designed program code was used. The obtained results showed that the quality of water has no impact on.   A series of novel antifungal triazole derivatives 2‐aryl‐1,2,4‐triazolo[1,5‐a]pyridine 9a–m were synthesized and tested in vitro for their growth inhibitory activities against C. albicans and T. MIC values indicate that the activities of three compounds were superior or comparable to fluconazole against both tested fungi, worthy of further investigation of its antifungal.